Method of making tantalum metal powder with controlled size distribution and products made therefrom

ABSTRACT

A process for sizing (i.e., comminuting) a tantalum powder including agglomerates of smaller particles, which process yields a tantalum powder having an as-comminuted agglomerate size distribution with the product of the Volume Mean Diameter, MV (in microns as measured by light scattering techniques such as Microtrac analysis), times specific surface area, BET (m 2  /g), being less than about 25. These powders after sizing typically have ratios of Scott Bulk Density : BET Surface Area in the range from about 20 to about 35. Also provided are powders having a substantially unimodal and narrow agglomerate size distribution in all stages of production, namely after sizing (i.e., deagglomeration by comminution), thermal agglomeration (i.e., heat treatment), and deoxidation. These resultant powders have high surface area and good flowability properties and, upon sintering, exhibit controlled shrinkage with high porosity. Further provided are sized heat treated tantalum powders having agglomerate particle sizes wherein the product of the Volume Mean Diameter, MV, times the specific surface area, BET, is in the range from about 90 to about 250. Sized and agglomerated powders which are deoxidized are also provided wherein the product of the Volume Mean Diameter, MV, times the specific surface area, BET, is in the range from about 90 to about 250.

FIELD OF THE INVENTION

This invention relates to a process of sizing tantalum metal powders, and to the powders produced thereby. More particularly, the invention relates to a process of sizing tantalum powder and to tantalum powder suitable for use in making sintered porous bodies, useful for example as capacitor electrodes.

BACKGROUND OF THE INVENTION

Among its many applications, tantalum powder is generally used to produce capacitor electrodes.

Tantalum capacitor electrodes, in particular, have been a major contributor to the miniaturization of electronic circuits. Such capacitor electrodes typically are manufactured by compressing agglomerated tantalum powder to less than half of the metal's true density with an electrode lead wire to form a pellet, sintering the pellet in a furnace to form a porous body (i.e., an electrode), and then subjecting the porous body to anodization in a suitable electrolyte to form a continuous dielectric oxide film on the sintered body. The anodized porous body is then impregnated with a cathode material, connected to a cathode lead wire and encapsulated.

The primary particle size and the agglomerated size (agglomerates are clusters of smaller primary particles), and the primary particle size and agglomerated size distributions of a powder, are important factors in the efficiency and efficacy of the subsequent sintering process by which porous bodies are made therefrom and in the electrical characteristics of the functional products, such as electrolytic capacitors, in which such porous bodies are incorporated.

In attempts to achieve a tantalum metal powder having the desirable characteristics for making capacitor electrodes and similar products, prior art powders were limited by the processes by which they were produced. Currently, for example, tantalum powders are generally produced via one of two methods: a mechanical process or a chemical process. The mechanical process includes the steps of electron beam melting of tantalum to form an ingot, hydriding the ingot, milling the hydride, and then dehydriding, crushing, and heat treating. This process generally produces powder with high purity, which is used in capacitor applications where high voltage or high reliability is required. The mechanical process suffers, however, from high production costs. In addition, tantalum powders produced by the mechanical process generally have low surface area.

The other generally utilized process for producing tantalum powder is a chemical process. Several chemical methods for producing tantalum powders suitable for use in capacitors are known in the art. U.S. Pat. No. 4,067,736, issued to Vartanian, and U.S. Pat. No. 4,149,876, issued to Rerat, disclose in detail the chemical production process involving sodium reduction of potassium fluorotantalate, K₂ TaF₇. A review of typical techniques is also described in the background sections of U.S. Pat. No. 4,684,399, issued to Bergman et al., and U.S. Pat. No. 5,234,491, issued to Chang.

Tantalum powders produced by chemical methods are well-suited for use in capacitors because they generally have larger surface areas than powders produced by mechanical methods. The chemical methods generally involve the chemical reduction of a tantalum compound with a reducing agent. Typical reducing agents include hydrogen and active metals such as sodium, potassium, magnesium, and calcium. Typical tantalum compounds include, but are not limited to, potassium fluorotantalate (K₂ TaF₇), sodium fluorotantalate (Na₂ TaF₇), tantalum pentachloride (TaCl₅), tantalum pentafluoride (TaF₅), and mixtures thereof. The most prevalent chemical process is the reduction of K₂ TaF₇ with liquid sodium.

The chemically reduced powder which results is referred to herein as "basic lot powder" and typically comprises agglomerates or clusters of smaller primary tantalum particles. These clusters or agglomerates are referred to herein as "basic lot agglomerates." The primary particle sizes of these basic lot agglomerates generally range from about 0.1 to about 5 microns in size. The size distribution for basic lot agglomerates for a conventional tantalum powder is shown in FIG. 1 as a comparative example. The basic lot agglomerate size distribution of basic lot powders is typically polydispersed and substantially bimodal. As defined herein, the term "polydispersed" means a broad distribution with a wide range of values and "bimodal" means a distribution with two modes (i.e., there are two different values which are conspicuously more frequent than neighboring values).

Basic lot powder is typically heat treated, milled, or crushed, and deoxidized such as by reaction with magnesium. The resultant product, sometimes referred to herein as a "heat treated and deoxidized powder" or "finished powder" typically includes some agglomerates, which may be referred to herein as "heat treated and deoxidized agglomerates."

Products of this type may be compressed and sintered to make porous bodies, such as anodes for capacitors. Capacitor electrodes produced from such heat treated and deoxidized powders of tantalum, however, suffer from non-uniform sintering and variable porosity distributions.

The process described above is generally illustrated by the schematic block diagram included as FIG. 15 hereof.

The resultant surface area of a finished tantalum powder is an important factor in the production of capacitors. The charge capability (CV) of a tantalum (for example) capacitor (typically measured as microfarad-volts) is directly related to the total surface area of the anode after sintering and anodization. Capacitors having high surface area anodes are desirable because the greater the surface area, the greater the charge capacity of the capacitor. Greater net surface area can be achieved, of course, by increasing the quantity (grams) of powder per pellet. One way to accomplish this is by pressing larger amounts of tantalum powder to form the porous pellet before sintering. This approach is restricted, however, because there is an inherent limit to the amount of powder which can be compacted into a given pellet size. Pellets pressed with higher than usual compression ratios result in anodes having poor porosity distributions with closed and non-uniform pores. Open, uniform pores are important for the steps of anodizing and impregnating the pellet to form the cathode.

As an alternative to increasing the quantity of tantalum powder used to produce the pellet, development efforts have focused on finding tantalum powders having higher specific surface areas. By increasing the specific surface area of these powders, higher surface area anodes having higher capacitance can be achieved while using smaller amounts of the tantalum powders. These higher capacitance values are typically measured based upon the volume of pellet produced (i.e., CV/cc). As a result, by using high surface area tantalum powders, capacitor sizes can be reduced while achieving the same level of capacitance. Alternatively, a larger capacitance can be achieved for a given capacitor size.

Various tantalum powder process techniques have been practiced which attempt to maximize the production of a powder having desired small primary particle sizes and, therefore, increased surface area. For example, U.S. Pat. No. 4,149,876, issued to Rerat, concerns techniques for controlling surface area of tantalum powder product in a reduction process wherein liquid sodium is added to a molten bath of K₂ TaF₇ and a diluent salt.

These various other tantalum powder process techniques which produce a powder having increased surface area still result, however, in a finished tantalum powder having a size distribution which is broad and polydispersed.

SUMMARY OF THE INVENTION

The present invention comprises a process for sizing a tantalum powder. The process comprises comminuting a tantalum powder having agglomerates comprising smaller primary particles, such as those produced by chemical reduction, prior to heat treatment (e.g., thermal agglomeration).

In one embodiment, the process of the present invention produces a tantalum powder including agglomerates of smaller particles, which process yields a tantalum powder having an as-comminuted agglomerate size distribution with the product of the Volume Mean Diameter, MV (in microns as measured by light scattering techniques such as Microtrac analysis), times specific surface area, BET (m² /g), being less than about 25.

In a preferred embodiment of the invention, the agglomerates are comminuted to yield a tantalum powder having an as-comminuted agglomerate size distribution within certain limits.

Preferably, the product produced according to the present invention is a tantalum powder having a relatively limited, more preferably unimodal, agglomerate size distribution in all stages of production, namely after sizing (i.e., deagglomeration by comminution), thermal agglomeration (i.e., heat treatment), and deoxidation. This resultant powder has high surface area, high purity, and good flowability properties and, upon sintering, exhibits controlled shrinkage with high porosity.

The present invention also includes sized heat treated basic lot tantalum metal powders having agglomerate particle sizes wherein the product of the Volume Mean Diameter, MV (expressed herein in micrometers), times the specific surface area, BET (expressed, herein, in square meters per gram), is in the range from about 90 to about 250. Sized and agglomerated powders of tantalum which are also deoxidized are also provided wherein the product of the Volume Mean Diameter, MV, times the specific surface area, BET, is in the range from about 90 to about 250.

This invention also encompasses sintered porous bodies made from powders treated in accordance with the present invention, capacitor electrodes made from such powders, and capacitors including such electrodes. Such electrodes and capacitors are as shown (except for the improvement of the present invention) in U.S. Pat. No. 5,217,526, of common assignment herewith, the essential disclosure of which is incorporated herein by reference. In one embodiment such capacitors may be made from basic lot powder treated in accordance with the present invention, at essentially any stage thereof, by techniques as referred and described in that patent at column 4, lines 28-50.

It is to be understood that both the foregoing general description and the following detailed description are exemplary, but are not restrictive, of the invention.

BRIEF DESCRIPTION OF THE DRAWING

The invention is best understood from the following detailed description when read in connection with the accompanying figures, in which:

FIG. 1 shows the narrow, substantially unimodal size distribution of basic lot agglomerates achieved by comminuting basic lot powders according to the present invention as compared with the polydispersed and substantially bimodal distribution of basic lot agglomerates in basic lot powders without comminution;

FIG. 2 shows the variation in basic lot size distributions according to a process of the present invention as a function of rotational speed of a Vortec milling apparatus as compared with the polydispersed distribution of basic lot agglomerates not treated in accordance with the present invention;

FIG. 3 shows the variation in Scott Bulk Densities of basic lot powders which are sized according to a process of the present invention as a function of rotational speed of a Vortec milling apparatus;

FIG. 4 shows the variation in heat treated and deoxidized agglomerate size distributions of finished powders achieved by thermally agglomerating and deoxidizing a sized basic lot powder according to a process of the present invention as compared with heat treated and deoxidized agglomerate size distributions of finished powders which result from thermally agglomerating and deoxidizing basic lot powders without sizing;

FIG. 5 shows the variation in the agglomerate size distribution of finished powders which were produced from basic lot powders sized according to a process of the present invention as a function of thermal agglomeration temperature;

FIG. 6 shows the variation in the agglomerate size distribution of finished powders produced by thermally agglomerating and deoxidizing basic lot powders sized according to a process of the present invention at 1250° C. for 30 minutes shown in FIG. 5, before and after screening;

FIG. 7 compares basic lot agglomerate size distributions of a basic lot powder which has been sized according to the present invention, before and after thermal agglomeration and deoxidation according to the present invention;

FIG. 8 shows the strength profiles of anodes produced using basic lot powders which have been sized, thermally agglomerated, and deoxidized according to the present invention;

FIG. 9 shows die fill rates of basic lot powders which have been sized, thermally agglomerated and deoxidized according to the present invention;

FIG. 10 shows the Scott Bulk Densities as a function of BET Surface Areas for basic lot powders which have been sized, thermally agglomerated, and deoxidized according to the present invention;

FIG. 11 shows die fill rates as a function of specific capacitance for basic lot powders which have been sized, thermally agglomerated, and deoxidized according to the present invention;

FIG. 12 shows the volumetric efficiency as a function of anode sintered density for basic lot powders which have been sized, thermally agglomerated, and deoxidized according to the present invention and for powders produced using conventional methods;

FIG. 13 shows a scanning electron micrograph of a basic lot tantalum powder without sizing which corresponds to Sample ID# A2-B;

FIG. 14 shows a scanning electron micrograph of a basic lot tantalum powder after sizing according to the present invention which corresponds to Sample ID# A2-BD;

FIG. 15 is a schematic block diagram illustrating a conventional process for producing high-surface area tantalum powder, suitable for making capacitor electrodes and other such articles, from a chemically reduced tantalum basic lot powder product comprising agglomerates of smaller tantalum particles; and

FIG. 16 is a schematic block diagram illustrating one embodiment of the process of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The size distribution ranges discussed below are defined as ranges between the D10 and D90 values of the particular powder being discussed, wherein the D10 and D90 values are defined as the size values at which 10 volume percent and 90 volume percent, respectively, of the particle/agglomerate diameters lie below.

The following testing procedures were used in the determination and evaluation of the analytical properties and the physical properties of the tantalum powders sized according to the process of the present invention. Surface area determinations of the tantalum powder were conducted using the nitrogen Brunauer, Emmett, Teller (BET) process using a Quantachrome Monosorb Surface Analyzer Model MS12. The purity of the tantalum powder was determined using spectrography by methods known in the art having a detection limit of 5 ppm for iron, nickel, chromium, and molybdenum.

All particle sizes discussed herein, except for Sample ID# A2-BDR, were measured by Microtrac analysis using a Leeds & Northrup Microtrac II Model 7998 analyzer without the use of a dispersant. The procedure comprised the steps of adding deionized water to the sample reservoir and then taking a background reading. The tantalum powder to be measured was added to the sample reservoir until the loading index window of the analyzer indicated a sample concentration of 0.88 +/-0.02 (T) at which time the particle size reading was taken and immediately reported. The particle size distribution for Sample ID# A2-BDU was measured by Microtrac analysis using a Leeds & Northrup Microtrac II Model 7998 as described above but with the particles dispersed using ultrasonic sound waves. The particle sizes of Sample ID# A2-BDR were measured using a Malvern Instruments MasterSizer X Ver. 1.2b.

The present invention is directed to the sizing of tantalum powders comprising agglomerates of smaller particles to produce a tantalum powder having an agglomerate size distribution with a Volume Mean Diameter times specific surface area (MV X BET) which is in the range from about 90 to about 250. The sized tantalum powders of the present invention are particularly adapted for use in capacitors. Preferably, the sized powders produced according to the present invention are tantalum powders having an agglomerate size distribution which is narrow, and more preferably unimodal.

In one embodiment the sizing process of the present invention comprises the step of taking a basic lot powder comprising tantalum having basic lot agglomerates and achieving an agglomerate size distribution which is narrow, at any point in the process prior to (immediately or otherwise) performing any heat treating or sintering operation. Preferably, this step is accomplished by comminuting a basic lot powder of tantalum to produce an as-comminuted powder having a comminuted agglomerate size from about 0.01 to about 20 micrometers with a median size of about 3 to 5 micrometers. These basic lot agglomerate sizes after comminution can be seen in FIG. 14 which is a scanning electron micrograph taken at a magnification of 15,000× of a basic lot powder of tantalum sized according to the Sample ID# A2-BD. As a comparison, FIG. 13 shows a scanning electron micrograph taken at a magnification of 15,000× of a basic lot powder of tantalum corresponding to Sample ID# A2-B which is not sized. It can be seen from these micrographs that powders sized according to the process of the present invention have much smaller and more uniform agglomerate sizes which comprise a smaller number of primary particles.

FIG. 1 shows the narrow and unimodal basic lot agglomerate size distribution achieved by the process of the present invention using a Waring Model 31BL40 high-speed laboratory blender as a high shear apparatus to accomplish wet comminution. FIG. 2 shows the narrow basic lot agglomerate size distribution achieved by the process of the present invention using a Vortec impact milling apparatus to accomplish dry comminution. These distributions permit the subsequent thermal agglomeration (i.e., heat treating) of powders and sintering of compacts to be done in a controlled fashion. According to the present invention, high shear comminution methods are most preferred because they produce powders having size distributions which are both narrow and unimodal as shown in FIG. 1. These high shear methods are accomplished using apparatus having high velocity blades which rotate at velocities sufficient to create mechanical and hydraulic shear stresses to break down metallurgically bonded particles. Typically, the tip velocities employed are from about 3000 to about 4000 feet per minute. Although less preferred, it is discovered that impact comminution methods according to the present invention are also effective because they produce powders having size distributions as shown in FIG. 2 which, although not entirely unimodal, are still narrow such that the attendant benefits discussed herein are realized.

FIG. 4 shows the agglomerate size distribution of a finished powder made by a conventional process (the "comparative example" curve) and the agglomerate size distribution of a finished powder made from sized basic lot powder according to the present invention (using a high shear mixer). The conventional process results in a polydispersed distribution whereas the process of the present invention results in a narrow distribution having a fine "tail" which constitutes a small volume percentage of the entire distribution. FIG. 7 shows the narrow basic lot agglomerate size distributions resulting from basic lot powders which have been sized according to the present invention and the narrow and unimodal agglomerate size distributions resulting from basic lot powders which have been sized, thermally agglomerated, and deoxidized according to the present invention.

As discussed above, in order to achieve uniform sintering and preserve maximum surface area, metal powders having narrow agglomerate size distributions are preferred with narrow and unimodal distributions being most preferred. In addition, because capacitor manufacturers press and sinter these powders into smaller pellet sizes, controlled shrinkage and porosity are important. It has been discovered that powders treated according to the present invention yield finished powders having a narrow, and more preferably a narrow and unimodal, size distribution which facilitates better control of sintering than conventional powders having a polydispersed size distribution. A unimodal size distribution is defined as those size distributions having profiles similar to those, for example, shown for the finished powders according to the present invention in FIGS. 4 and 5.

Because shrinkage is a function of particle diameter, powders with wide particle size distributions typically result in varying amounts of shrinkage in an anode which can result in a large degree of non-uniformity and closed pores. It is theorized that, because the powders have narrow particle size distributions, uniform shrinkage would result in anodes produced from these powders. Thus, capacitors produced from powders made according to the present invention should exhibit controlled shrinkage with high porosity and uniform pore size distribution as compared with capacitors produced using conventional polydispersed tantalum powders.

The comminution process of the present invention is performed by subjecting a tantalum powder comprising agglomerates of smaller particles to high shear or impact stresses under either wet or dry conditions. The following examples illustrate both wet and dry comminuting methods according to the present invention. It is to be understood that, although the preferred metal powders to be sized are basic lot powders of tantalum produced by a chemical reduction process, it is contemplated that other metal powders produced by other methods can be sized by the process as disclosed herein. Thus, the present invention is not limited to the particular examples set forth below, but can be used in conjunction with other metal powders as will be readily ascertainable to a person having ordinary skill in the art.

The basic lot powders of tantalum to be sized in the following examples, i.e., the agglomerates of smaller particles produced directly upon chemical reduction, were produced using a conventional sodium reduction process as discussed in the background section above. The basic lot agglomerates generally fell into two primary particle size ranges, each having a polydispersed, substantially bimodal basic lot agglomerate size distribution. Five basic lot powders having high surface areas (labelled as lots A1, A2, A3, A4, and A5) were prepared having basic lot agglomerate size distributions ranging from about 2 to about 132 microns. To determine the effect of primary particle sizes in the basic lot powders, a sixth basic lot powder (labelled as B1) was also prepared which had a basic agglomerate size distribution ranging from about 5 to about 95 microns. The size distributions and Scott density data for these basic lot powders are shown in Table 2.

It is to be understood that, although the particle size distribution data and the figures are shown having a lower limit of "1," the present invention is not intended to be limited thereby. This is due to the inability of the Leeds & Northrup Microtrac II Model 7998 to measure particle sizes smaller than 1 micrometer. Sample A2-BDR measured using the Malvern Instruments MasterSizer X Ver. 1.2b (capable of measuring down to 0.02 micrometers) is provided as an example which illustrates the lower size ranges which can be achieved by the present invention. The basic lot powders were then divided into sample lots and comminuted as described below.

I. WET COMMINUTION METHODS

A) Wet Comminution Using a Waring Laboratory Blender

One hundred gram samples of basic lot powders A3 and A4 were each separately mixed with 500 ml of cold (i.e., room temperature), deionized water and comminuted in a Waring Model 31BL40 high-speed laboratory blender. The powder and water mixtures were comminuted at the highest rpm setting (20,000 rpm) for 10 minutes. This process was repeated until 50 lbs of sized powder were produced. The resultant sheared powder was then filtered, acid leached, rinsed, dried, and divided into samples which were then heat treated at different thermal agglomeration temperatures. The heat treatment cycles used on samples taken from lot A3 (Sample ID# A3-BD) were 1200° C. for 60 minutes (Sample ID# A3-BDH1), 1250° C. for 60 minutes (Sample ID# A3-BDH2), and 1350° C. for 60 minutes (Sample ID# A3-BDH3). A sample from lot A4 (Sample ID# A4-BD) was heat treated at 1230° C. for 60 minutes (Sample ID# A4-BDH1). Properties of the basic lot powders before and after heat treatment are shown in Table 2 with derived parameters being tabulated in Table 3.

B) Wet Comminution Using a Ross Laboratory High-Shear Model 100 LC Mixer

Two thousand five hundred ml of cold, deionized water were placed in a one-liter, stainless steel beaker. The stainless steel beaker was then placed in an ice bath and under the rotor of a Ross 100 LC mixer set at 500 rpm. One thousand grams of each of basic lot powders A1 and B1 were slowly added to the deionized water while mixing at 500 rpm. The mixer speed was increased to the highest setting (10,000 rpm) and blended for a total of about 60 minutes. Ice was continually added to keep the bath cold. The powder was then filtered, leached with a mixture of acids (e.g., dilute aqua regia) to remove any contaminants, and dried.

The resultant sheared powders were then divided into samples which were heat treated at different thermal agglomeration temperatures. The heat treatment cycles used on samples taken from lot B1 (Sample ID# B1-BD) were 1400° C. for 30 minutes (Sample ID# B1-BDH3) and 1500° C. for 30 minutes (Sample ID# B1-BDH4). A sample from lot A1 (Sample ID# A1-BD) was heat treated at 1200° C. for 30 minutes (Sample ID# A1-BDH1). Properties of the basic lot powders before and after heat treatment are shown in Table 2 with derived parameters being tabulated in Table 3.

C. Wet Comminution Using a Commercial Grade Ross Model 105ME High Shear Mixer

Ten gallons of deionized water were placed in a container under the rotor of a Ross 105 ME/mixer set at 500 rpm. Fifty pounds of basic lot powder A2 were slowly added to the deionized water while mixing at the highest speed (about 3000 rpm, which corresponds to a tip speed of 3500 feet per minute). Blending was continued for a total of about 90 minutes at which time the water was decanted and the powder filtered. The powder was then washed with a mixture of acids to remove any contaminants.

The resultant sheared powder was then filtered, dried, and divided into samples which were then heat treated at different thermal agglomeration temperatures. The heat treatment cycles used on samples from lot A2 (Sample ID# A2-BD) were 1250° C. for 30 minutes (Sample ID# A2-BDH1) and 1350° C. for 30 minutes (Sample ID# A2-BDH2). Properties of the basic lot powder before and after heat treatment are shown in Table 2 with derived parameters being tabulated in Table 3. For basic lot powder A2, the particle size distribution for Sample ID# A2-BD was measured by a standard Microtrac analysis which measures the scattering of a laser light directed through a suspension of the powder in water.

D. Ball Milling of a Wet Basic Lot Powder

A one-gallon ball mill was filled half full with 1/2-inch diameter stainless steel balls. Six hundred ml of water and 285 g of basic lot powder were then added. The ball mill was then tumbled for 16 hours and the resultant tantalum powder was washed and filtered.

II. DRY COMMINUTION METHODS

A water-washed, acid-leached, and dried basic lot powder A5, made according to a conventional sodium reduction process, was obtained. A powder was selected having a high hydrogen concentration (preferably above 1500 ppm although powders having lower concentrations may be used) so that it was brittle. The data for this starting basic lot powder is shown below in Table 1. The basic lot powder was milled by single-pass Vortec milling in an M1 mill with product collected in a cyclone recovery system. Five pound lots of the A5 basic lot powder were processed at each of the following selected machine speeds: 5,000; 7,500; 10,000; 15,000; and 20,000 rpm.

The Scott density, oxygen content, D10, D50, D90, and Volume Mean Diameter (MV) data of the Vortec-milled samples are shown in Table 1 below:

                  TABLE 1     ______________________________________                     Scott  D10    D50   D90    MV     ID     RPM      g/in.sup.3                            microns                                   microns                                         microns                                                microns     ______________________________________     A5-B   Starting 15.2   3.03   20.95 81.29  32.31            Basic Lot     A5-BD1  5000    18.8   2.13   6.56  37.21  13.21     A5-BD2  7500    22.7   2.02   4.96  21.48  9.34     A5-BD3 10000    21.1   1.81   3.68  15.68  7.11     A5-BD4 15000    24.0   1.71   3.54  15.91  6.64     A5-BD5 20000    27.5   1.44   2.87  9.92   4.26     ______________________________________

The size distribution ranges for these Vortec-milled powders are shown in FIG. 2 with the Scott densities illustrated in FIG. 3.

Although the process of the present invention is illustrated using the various comminution methods described above, it is envisioned that other comminution methods such as ultrasonic milling and jet milling can also be employed.

III. DEOXIDATION OF THE COMMINUTED AND HEAT TREATED LOTS

Samples were taken from each of comminuted and heat-treated basic lot powders from lots A1, A2, A3, A4, and B1 and subjected to a magnesium deoxidation treatment. In this treatment a small amount of magnesium metal powder (i.e., 1-2 weight percent) is blended with the heat treated tantalum powder. The mixture is heated from about 800 to about 1000° C. to react the magnesium with and reduce the oxygen contained in the finished tantalum powder. The tantalum powder is subsequently leached and dried. The raw data corresponding to these powders in all stages of production (i.e., for the as-reduced basic lot powder, after sizing, after heat treating, and after deoxidizing) are shown in Table 2 below. Derived parameters are shown in Table 3.

The sample identification numbers in the tables consist of a prefix which refers to the basic lot powder number and a suffix indicating the treatments performed on the tantalum powders. The identification numbers are abbreviated as follows:

B=a basic lot powder;

BD=a basic lot powder which has been sized;

BDH#=a basic lot powder which has been sized and heat treated (the heat treatment # is carried throughout the subsequent processing steps to the sample);

BDH#M=a basic lot powder which has been sized, heat treated, and deoxidized;

BDH#MS=a basic lot powder which has been sized, heat treated, deoxidized, and screened to about 500 mesh; and

BH#M=a basic lot powder which has been heat treated and deoxidized.

Thus, as an example, sample ID# A4-BDH1M is a basic lot powder from lot A4 which has been sized, heat treated at 1230° C. for 60 minutes, and deoxidized.

                                      TABLE 2     __________________________________________________________________________                     BET D10                            D50 D90 MV  Die Fill                                            Scott              Sample ID                     m 2/g                         μm                            μm                                μm                                    μm                                        mg/s                                            g/in 3     __________________________________________________________________________     Basic Lot              A1-B   1.13                         2.61                            13.86                                69.26                                    25.43   17     Basic Lot              A2-B   1.17                         3.31                            26.28                                93.64                                    37.68   16     Basic Lot              B1-B   0.95                         5.14                            33.56                                95.31                                    42.20   19     Basic Lot              A3-B   1.14                         3.27                            21.55                                79.09                                    32.15   13     Basic Lot              A4-B   1.32                         3.20                            33.26                                131.88                                    53.05   14     DA Ross 100LC              A1-BD  1.14                         1.77                            3.67                                13.58                                    5.91    33     DA Ross 105ME              A2-BD  1.18                         2.14                            5.33                                18.41                                    8.75    32     DA Ross 105ME              A2-BDU 1.18                         1.39                            2.94                                10.28                                    4.52    32     DA Ross 100LC              B1-BD  0.99                         2.04                            5.81                                15.53                                    7.39    32     DA Waring              A3-BD  1.10                         1.81                            3.44                                10.53                                    5.41    31     DA Waring              A4-BD  1.33                         1.83                            3.54                                9.89                                    4.86    25     DA Ross 105ME              A2-BDR 1.18                         0.19                            0.41                                0.98                                    0.41     HT 1200 C 30 min              A1-BDH1                     0.92                         10.32                            201.56                                347.14                                    193.13  38     HT 1250 C 30 min              A2-BDH1                     0.70                         7.58                            111.69                                299.71                                    129.58  27     HT 1350 C 30 min              A2-BDH2                     0.51                         13.62                            135.56                                300.05                                    142.32  33     HT 1400 C 30 min              B1-BDH3                     0.47                         10.47                            132.39                                301.55                                    138.29  42     HT 1500 C 30 min              B1-BDH4                     0.33                         17.83                            158.38                                326.34                                    162.97  49     HT 1200 C 60 min              A3-BDH1                     0.89                         3.61                            107.77                                286.50                                    122.56  28     HT 1250 C 60 min              A3-BDH2    43.54                            204.71                                345.33                                    200.67  34     HT 1350 C 60 min              A3-BDH3                     1.22                   38     HT 1230 C 60 min              A4-BDH1    4.68                            101.39                                289.86                                    121.50  26     Deoxidized              A1-BDH1M                     1.07                         11.71                            203.74                                346.79                                    198.24                                        142 48     Deoxidized              A2-BDH1M                     0.71                         8.26                            156.63                                329.59                                    156.89                                        25  35     Deoxidized              A2-BDH2M                     0.60                         12.04                            159.41                                314.09                                    157.19                                        80  41     Deoxidized              B1-BDH3M                     0.55                         10.77                            137.89                                327.98                                    149.97                                        142 45     Deoxidized              B1-BDH4M                     0.42                         21.74                            190.31                                356.62                                    190.17                                        302 52     Deoxidized              A3-BDH1M                     0.96                         46.46                            207.90                                339.10                                    202.48                                        63  38     Deoxidized              A3-BDH2M                     0.92                         44.9                            192.64                                331.1                                    190.73                                        160 40     Deoxidized              A3-BDH3M                     0.68                         73.43                            202.92                                335.94                                    203.65                                        632 47     Deoxidized              A4-BDH1M                     1.07                         5.89                            142.92                                316.67                                    146.99  31     Screened A3-BDH1MS  85.16                            212.55                                342.1                                    214.29                                        345     Screened A3-BDH2MS  84.92                            199.96                                333.94                                    204.14                                        634     __________________________________________________________________________

                  TABLE 3     ______________________________________                                 Flow/              Sample ID                       BET X MV  BET     Scott/BET     ______________________________________     Basic Lot  A1-B       29              15     Basic Lot  A2-B       44              14     Basic Lot  B1-B       40              20     Basic Lot  A3-B       37              11     Basic Lot  A4-B       70              11     DA Ross 100LC                A1-BD      7               29     DA Ross 105ME                A2-BD      10              27     DA Ross 105ME                A2-BDU     5               27     DA Ross 100LC                B1-BD      7               32     DA Waring  A3-BD      6               28     DA Waring  A4-BD      6               19     DA Ross 105ME                A2-BDR     0.48     HT 1200 C 30 min                A1-BDHl    178     HT 1250 C 30 min                A2-BDH1    91     HT 1350 C 30 min                A2-BDH2    73     HT 1400 C 30 min                B1-BDH3    65     HT 1500 C 30 min                B1-BDH4    54     HT 1200 C 60 min                A3-BDH1    109     HT 1250 C 60 min                A3-BDH2     HT 1350 C 60 min                A3-BDH3     HT 1230 C 60 min                A4-BDH1     Deoxidized A1-BDH1M   212       133   45     Deoxidized A2-BDH1M   111       35    49     Deoxidized A2-BDH2M   94        133   68     Deoxidized B1-BDH3M   82        258   82     Deoxidized B1-BDH4M   80        719   124     Deoxidized A3-BDH1M   194       66    40     Deoxidized A3-BDH2M   183       167   42     Deoxidized A3-BDH3M   138       929   69     Deoxidized A4-BDH1M   135     Screened   A3-BDH1MS     Screened   A3-BDH2MS     ______________________________________

Table 4 below tabulates the properties of comparative basic lot powder samples of tantalum which are not sized. These samples were produced by the conventional sodium reduction process of potassium fluorotantalate (K₂ TaF₇) as described above. Table 5 below shows derived parameters of these comparative samples produced by the conventional powder process without comminution.

                  TABLE 4     ______________________________________            D10    D50     D90   MV    BET   Scott Flow     ID     μm  μm   μm μm m 2/g g/in 3                                                   mg/s     ______________________________________     E1-BHM 16.32  66.25   203.42                                 88.10 0.48     E2-BHM 16.19  60.83   186.35                                 82.86 0.48     E3-BHM 17.03  65.26   187.64                                 86.11 0.48     E4-BHM 15.97  60.67   173.11                                 79.82 0.48     D1-BHM 15.62  63.05   183.27                                 83.69 0.65     D2-BHM 17.78  74.88   218.59                                 96.22 0.65     D3-BHM 14.43  59.09   166.74                                 76.79 0.65     D4-BHM 15.44  70.75   258.86                                 105.93                                       0.65     D5-DHM 15.60  60.62   234.64                                 94.80 0.65     D6-DHM 18.14  73.83   206.59                                 92.87 0.65     C1-BHM 13.29  57.88   207.18                                 84.06 0.45     C2-BHM 11.59  46.63   140.04                                 61.77 0.45     C3-BHM 13.19  54.82   179.08                                 78.26 0.45     C4-BHM 13.02  53.82   178.02                                 77.19 0.45     B2-BHM 10.75  46.40   153.56                                 65.50 0.66     B3-BHM 10.77  48.21   164.18                                 69.77 0.66     B4-BHM 10.81  47.87   162.79                                 69.14 0.66     B5-BHM 9.98   42.36   161.64                                 65.81 0.66     B6-BHM 10.62  47.54   174.59                                 71.40 0.66     B7-BHM 10.71  49.00   190.63                                 75.12 0.66     A5-BH1M            9.44   44.31   202.52                                 75.82 0.82  24.58 61     A5-BH1M            8.98   44.39   204.32                                 76.19 0.87  26.71 66     A5-BH2M            10.04  44.02   174.78                                 71.31 0.65  27.19 80     A5-BH2M            10.21  62.41   259.05                                 101.93                                       0.82  27.83 96     A5-BH3M            11.81  64.22   240.37                                 97.74 0.68  34.83 137     A5-BH3M            16.08  95.97   283.58                                 123.93                                       0.61  40.42 251     A5-BH4M            15.24  107.35  290.80                                 130.06                                       0.52  41.26 186     A5-BH4M            13.96  76.85   243.71                                 104.75                                       0.56  43.81 244     A5-BH1M            9.44   50.64   204.68                                 79.76 0.74  30.91 107     A5-BH1M            10.87  62.58   247.03                                 99.24 0.85  29.01 95     A5-BH2M            11.13  49.67   199.15                                 77.61 0.67  32.31 137     A5-BH2M            10.92  57.39   233.37                                 92.66 0.71  32.84 132     A5-BH3M            16.67  108.95  281.18                                 128.57                                       0.61  39.69 209     A5-BH3M            12.27  54.99   216.16                                 84.70 0.54  44.78 263     A5-BH4M            20.67  108.85  301.13                                 134.72                                       0.46  49.39 338     A5-BH4M            27.04  145.72  322.44                                 159.47                                       0.52  44.92 386     ______________________________________

                  TABLE 5     ______________________________________     ID       MV*BET       Scott/BET                                    Flow/BET     ______________________________________     E1-BHM   42     E2-BHM   40     E3-BHM   41     E4-BHM   38     D1-BHM   54     D2-BHM   63     D3-BHM   50     D4-BHM   69     D5-DHM   62     D6-DHM   60     C1-BHM   38     C2-BHM   28     C3-BHM   35     C4-BHM   35     B2-BHM   43     B3-BHM   46     B4-BHM   46     B5-BHM   43     B6-BHM   47     B7-BHM   50     A5-BH1M  62           30       75     A5-BH1M  66           31       76     A5-BH2M  46           42       123     A5-BH2M  84           34       117     A5-BH3M  66           51       202     A5-BH3M  76           66       412     A5-BH4M  68           79       357     A5-BH4M  59           78       436     A5-BH1M  59           42       144     A5-BH1M  84           34       112     A5-BH2M  52           48       205     A5-BH2M  66           46       186     A5-BH3M  78           65       343     A5-BH3M  46           83       486     A5-BH4M  62           107      736     A5-BH4M  83           86       743     ______________________________________

The data of Tables 1, 2, 3, 4, and 5 were used to prepare the graphs of FIGS. 1 to 7 which illustrate the tantalum powders having a narrow agglomerate size distribution in all phases of production.

With regard to the powders subjected to comminution by Vortec milling, analysis of the samples shows that single-pass Vortec milling reduced the basic lot agglomerate size while increasing the Scott density. The comparison of before and after Microtrac analyses is provided in FIG. 2 which shows a shift towards finer basic lot agglomerate sizes after comminution as the rotational speed is increased. As a specific example, comparing the Microtrac analysis of the basic lot powder sample without sizing and the basic lot powder sample sized at 20,000 rpm reveals a size distribution peak at about three microns with virtually no particles larger than 30 microns after Vortec milling whereas the basic lot without sizing shows substantial numbers of agglomerates at 100 microns or greater. The Scott densities achieved after Vortec milling are shown in FIG. 3.

It is observed that Vortec milling is capable of comminuting the large basic lot agglomerates of basic lot powders of tantalum without adversely affecting powder chemistry. Further advantages of the process of the present invention and the powders which result are discussed below.

IV. BASIC LOT CHEMICAL PURITY

Basic lot powders of tantalum produced by the reduction of K₂ TaF₇ by sodium in the presence of diluent salts typically have trapped impurities such as Fe, Ni, Na⁺ and K⁺. These impurities are detrimental to the electrical performance of tantalum capacitors. Because the sizing process of the present invention breaks down larger basic lot agglomerates, it is believed that trapped impurities are released thereby producing high purity tantalum powders.

V. IMPROVEMENTS IN THE FLOW OF FINISHED POWDER

The powders made using the process of the present invention show a dramatic improvement in flowability because of their agglomerate size distribution. In the finished stage, powders produced using conventional methods have a polydispersed distribution as seen in FIG. 4. The finished powders made using the process of the present invention have a substantially unimodal, narrow distribution after sizing, heat treatment, and deoxidation as can be seen in FIG. 4. FIG. 5 shows the effect of varying the heat treatment temperatures in producing the finished powders according to the present invention.

The flowability of finished (heat treated and deoxidized) powders was measured by a die fill test. This test very closely mimics the conditions under which capacitor manufacturers use tantalum powder. A hopper filled with 40 g of tantalum powder is passed over 10 holes with 0.125-inch diameter which are spaced 1 inch from each other in a row using an even 2 second pass. The weight of the powder that fills the 10 holes is measured after each pass. This process is continued until the hopper is empty. The average rate in mg/s is computed by regression analysis. For high capacitance powders a die fill rate of 130 to 150 mg/s is preferable with higher die fill rates being more preferred. Table 7 below compares the die fill flow rate of powders made with the present invention and conventional powder. Because the die fill rate depends on the specific charge of the powder (it is lower for powders with high specific charge), powders with similar specific charge are compared in Table 6 and graphed in FIG. 11. The die flow rates are also graphed at varying BET values in FIG. 9.

                  TABLE 6     ______________________________________              Specific Charge        Die Fill Rate after              (CV/g)      Die Fill Rate                                     screening 20%*     Powder   1F-V/g      mg/s       mg/s     ______________________________________     Comparative              37900       50          86     Example     A3-BDH1M 39671       160        --     A3-BDH1MS              39671       --         634     A3-BDH2M 40455       63         --     A3-BDH2MS              40455       --         345     Comparative     Example  34000       55         125     A3-BDH3M 31985       632        Insufficient fines to                                     screen     ______________________________________      (*): -500 Mesh removed via screening

For conventional powders, one way to improve the flow has been screening out fines. Such improvements are only modest, however, as seen in Table 6 above. The effect of screening the powders produced by the process of the present invention was also evaluated. It is discovered that the flow performance of the comminuted powders of the present invention can be improved by a small amount of screening. Table 6 above shows the flow improvement obtained by screening on an as-comminuted particle size distribution. The fine "tail" of this distribution can be removed by screening, leaving behind a true unimodal and narrow particle size distribution, as shown in FIG. 6, with greatly enhanced flow.

An additional advantage is realized in the yield which results when screening finished powders according to the present invention. As can be seen from FIG. 4, which shows the size distributions of unscreened finished powders, because finished powders according to the present invention have a fine "tail" which constitutes a small volume percentage of the entire distribution, a larger yield of usable powder remains after screening. In contrast, the process of screening a conventional finished powder having a polydispersed size distribution removes a larger amount of powder when screened to the same mesh sizes. Furthermore, even after screening a conventional powder to the same mesh size, the size distribution of the remaining powder is still not as narrow as that which results from screened powders according to the present invention.

VI. CAPACITORS COMPRISING POWDERS MADE ACCORDING TO THE PRESENT INVENTION

The specific charge of a powder is an important aspect of a powder which is to be used in the manufacture of capacitors. Although specific charge is commonly denoted by the designation "CV/cc" and is expressed in units of "μF-V/cc," those skilled in the art will recognize that the designation "CV/g," commonly used by powder manufacturers, may also be utilized and that designation is expressed in units of "μF-V/g."

In order to evaluate the performance of the powders of the present invention, rectangular capacitor anodes (3.21 mm×3.21 mm×1.36 mm and 70 mg) were produced by compressing tantalum powder produced in accordance with the present invention into pellets, with wire electrodes, to a density of between 5 to 7 g/cc green density and sintering the pellets at a temperature between 1300 to 1500° C. for 10 minutes under vacuum to produce a porous sintered body having uniform open pores. The porous body was then anodized by submersing the body in 0.1 volume % phosphoric acid while applying a voltage of 50 to 100 volts. The anodes, after anodizing, rinsing, and drying, were first tested for electrical leakage. A 10 volume % phosphoric acid test solution was used. The anodes were immersed in the test solution to the top of the anode and a voltage of 70% of the final formation voltage (i.e., 35 volts if it was anodized at 50 volts) was applied for 2 minutes after which the electrical leakage was measured. After the electrical leakage measurements were completed, the specific charge was measured on the anode employing a type 1611B General Radio Capacitance Test Bridge. The capacitors produced from powders according to the present invention using a 50 V formation voltage typically ranged from 20,000 μF-V to 50,000 μF-V.

Comparative capacitor anode samples were produced by the same process using the comparative samples of Tables 4 and 5. The physical and electrical properties of the capacitors produced using conventional powders and the powders of the present invention were evaluated. FIGS. 8 and 12 graphically represent this data and serve to further explain the present invention with regard to the effect of sizing the tantalum powders. FIG. 8 shows the green strength of the anodes to be 25 lbs and above when pressed at or above a press density of 6.0 g/cc. This green strength is adequate for capacitor manufacturing.

FIG. 12 compares the volumetric efficiency of an anode made from a powder according to the present invention with a conventional powder having a similar specific charge (CV/g). The powders of the present invention have higher volumetric efficiencies than conventional powders. It is believed that this is the result of the unique combination of high bulk density and high specific charge of the powders of the present invention. The porosity distribution of the powders of the present invention when pressed to a press density of 6.5 g/cc is the same as that obtained when pressing a conventional powder from which approximately 45 volume % of the powder has been screened using a 325 mesh screen at the same press density. Thus, higher volumetric efficiencies are achieved over the conventional powders. It is believed that conventional powders, if not screened, cannot be pressed to such press densities. Typically, conventional powders are only pressed to press densities of 5 to 5.5 g/cc.

VII. BETTER VOLUMETRIC EFFICIENCY

For high capacitance powders, a critical parameter is the charge per unit volume. Capacitor manufacturers can meet the charge requirements using a smaller case size if powder manufacturers can provide high CV/cc powders. Powders made according to the present invention have higher bulk density (1.25 to 3.44 g/cc or 20 to 55 g/in³) than conventional powders having similar surface areas made using conventional processes (1.25 to 1.6 g/cc or 20 to 25.6 g/in³). See FIGS. 10 and 11. Consequently, for similar specific surface areas, powders made according to the present invention can be pressed to higher densities using the same pressing ratio. If conventional powders with low bulk densities and irregular size distributions are pressed to high green densities, pore closure results and, consequently, surface area and capacitance are reduced. The invention powders can be used at high press densities such as 6.5 and 7.0 g/cc while conventional powders can reasonably be used at 5.0 to 5.5 g/cc.

This improvement in electrical performance is best illustrated in FIG. 12 which clearly shows that, for comparable specific charge, the powders made according to the present invention have higher CV/cc values than conventional powders.

VIII. LEAKAGE DATA

Shown in Table 7 below are electrical leakage data of capacitors made from powders according to the present invention. Table 8 shows comparative leakage data of capacitors produced from conventional powders sintered at 1400° C. for 30 minutes for samples A6-BHM; 1425° C. for 30 minutes for samples B8-BHM; and 1450° C. for 30 minutes for samples A8-BHM. Upon comparing capacitors having similar capacitance values, those produced from invention powders have similar leakage values even when lower sintering temperatures are used. For example, a capacitor having a capacitance of 230,587 CV/cc produced by pressing powder Sample ID# A3-BDH2M of the present invention to a press density of 5.0 g/cc, sintering at 1250° C. for 60 minutes, and then forming a dielectric using a formation voltage of 50 volts has a DC leakage of 8.81 (μA/g). This is comparable to the DC leakage of 8.34 (μA/g) obtained by a capacitor having a capacitance of 219,218 CV/cc produced by pressing comparative powder Sample ID# A6-BHM to a press density of 5.0 g/cc, sintering at 1400° C. for 30 minutes, and then forming a dielectric using a formation voltage of 50 volts.

                                      TABLE 7     __________________________________________________________________________     Electrical Properties of Invention Powders           Press               Sinter     Capacitance                                Capacitance                                      DC Leakage                                            DC Leakage     Sample           Density               Temperature                     Formation                          (CV/g)                                (CV/cc)                                      (uA/g)                                            (nA/CV)     ID    g/cc               C.    Voltage                          μF-V/g                                μF-V/cc                                      (uA/g)                                            (nA/μF-V)     __________________________________________________________________________     A3-BDH3M           5.0 1335  50 V 37,781                                193,336                                      8.51  0.23     A3-BDH3M           5.3 1335  50 V 37,315                                204,339                                      6.92  0.19     A3-BDH3M           5.6 1335  50 V 36,630                                206,231                                      6.45  0.18     A3-BDH3M           5.9 1335  50 V 35,972                                218,161                                      6.79  0.19     A3-BDH3M           6.2 1335  50 V 35,496                                228,546                                      6.77  0.19     A3-BDH3M           6.5 1335  50 V 34,649                                235,006                                      6.47  0.19     A3-BDH3M           6.8 1335  50 V 33,907                                240,481                                      5.86  0.17     A3-BDH3M           5.0 1405  50 V 31,985                                178,636                                      3.05  0.10     A3-BDH3M           5.3 1405  50 V 32,188                                197,826                                      3.92  0.12     A3-BDH3M           5.6 1405  50 V 30,838                                193,516                                      3.21  0.10     A3-BDH3M           5.9 1405  50 V 30,631                                208,434                                      3.21  0.10     A3-BDH3M           6.2 1405  50 V 30,323                                215,536                                      3.12  0.10     A3-BDH3M           6.5 1405  50 V 29,461                                223,563                                      3.01  0.10     A3-BDH3M           6.8 1405  50 V 28,653                                224,043                                      2.93  0.10     A3-BDH2M           5.0 1335  50 V 44,379                                230,587                                      8.81  0.20     A3-BDH2M           5.3 1335  50 V 43,745                                240,597                                      9.73  0.22     A3-BDH2M           5.6 1335  50 V 42,909                                251,414                                      10.00 0.23     A3-BDH2M           5.9 1335  50 V 41,823                                259,480                                      11.18 0.27     A3-BDH2M           6.2 1335  50 V 40,903                                267,635                                      9.27  0.23     A3-BDH2M           6.5 1335  50 V 39,957                                273,538                                      9.37  0.23     A3-BDH2M           6.8 1335  50 V 38,834                                277,314                                      7.78  0.20     A3-BDH2M           5.0 1405  50 V 39,671                                225,480                                      5.43  0.14     A3-BDH2M           5.3 1405  50 V 38,457                                238,294                                      5.26  0.14     A3-BDH2M           5.6 1405  50 V 38,341                                245,951                                      4.46  0.12     A3-BDH2M           5.9 1405  50 V 36,599                                253,667                                      5.99  0.16     A3-BDH2M           6.2 1405  50 V 35,384                                255,670                                      4.58  0.13     A3-BDH2M           6.5 1405  50 V 34,213                                259,599                                      4.70  0.14     A3-BDH2M           6.8 1405  50 V 33,440                                264,503                                      4.43  0.13     A3-BDH1M           5.0 1335  50 V 48,522                                254,164                                      9.11  0.19     A3-BDH1M           5.3 1335  50 V 44,993                                249,621                                      15.29 0.34     A3-BDH1M           5.6 1335  50 V 44,031                                259,173                                      7.63  0.17     A3-BDH1M           5.9 1335  50 V 42,840                                269,655                                      8.55  0.20     A3-BDH1M           6.2 1335  50 V 42,138                                275,377                                      9.53  0.23     A3-BDH1M           6.5 1335  50 V 40,528                                283,633                                      7.35  0.18     A3-BDH1M           6.8 1335  50 V 39,560                                288,373                                      11.85 0.30     A3-BDH1M           5.0 1405  50 V 40,455                                236,047                                      4.58  0.11     A3-BDH1M           5.3 1405  50 V 39,628                                243,384                                      5.09  0.13     A3-BDH1M           5.6 1405  50 V 38,564                                254,105                                      4.21  0.11     A3-BDH1M           5.9 1405  50 V 37,257                                260,455                                      5.15  0.14     A3-BDH1M           6.2 1405  50 V 36,691                                260,742                                      4.48  0.12     A3-BDH1M           6.5 1405  50 V 34,601                                268,759                                      3.98  0.12     A3-BDH1M           6.8 1405  50 V 33,623                                270,767                                      4.24  0.13     A1-BDH1M           6.0 1360  50 V 43,601                                277,392                                      9.03  0.21     A1-BDH1M           6.0 1440  50 V 35,949                                263,272                                      5.43  0.15     A1-BDH1M           6.0 1360  70 V 37,497                                239,325                                      13.35 0.36     A1-BDH1M           6.0 1440  70 V 30,868                                223,802                                      8.29  0.27     B1-BDH3M           6.0 1360  50 V 28,220                                175,130                                      4.62  0.16     B1-BDH3M           6.0 1360  70 V 25,668                                158,614                                      8.48  0.33     B1-BDH3M           6.0 1440  50 V 25,593                                167,204                                      3.62  0.14     B1-BDH3M           6.0 1440  70 V 23,700                                152,069                                      4.97  0.21     B1-BDH4M           6.0 1440  50 V 20,786                                129,444                                      3.01  0.15     B1-BDH4M           6.0 1440  70 V 19,495                                121,123                                      3.18  0.17     B1-BDH4M           6.0 1360  70 V 20,332                                122,442                                      5.26  0.26     B1-BDH4M           6.0 1360  50 V 21,880                                131,275                                      4.14  0.19     __________________________________________________________________________

                                      TABLE 8     __________________________________________________________________________     Electrical Properties of Prior Art and Comparative Example Powders           Press               Sinter     Capacitance                                Capacitance DC Leakage     Sample           Density               Temperature                     Formation                          (CV/g)                                (CV/cc)                                      DC Leakage                                            (nA/CV)     ID    g/cc               C.    Voltage                          μF-V/g                                μF-V/cc                                      (uA/g)                                            (nA/μF-V)     __________________________________________________________________________     A6-BHM           5.0 1335  50 V 40,268                                203,417                                      5.97  0.15     A6-BHM           5.3 1335  50 V 39,725                                211,395                                      5.46  0.14     A6-BHM           5.6 1335  50 V 39,110                                220,081                                      6.23  0.16     A6-BHM           5.9 1335  50 V 38,366                                227,477                                      6.36  0.17     A6-BHM           6.2 1335  50 V 37,704                                234,021                                      6.72  0.18     A6-BHM           6.5 1335  50 V 36,885                                241,628                                      5.55  0.15     A6-BHM           6.8 1335  50 V 35,903                                247,273                                      5.15  0.14     A6-BHM           5.0 1405  50 V 37,900                                203,744                                      3.92  0.10     A6-BHM           5.3 1405  50 V 37,419                                209,682                                      3.6   0.10     A6-BHM           5.6 1405  50 V 36,780                                217,772                                      3.7   0.10     A6-BHM           5.9 1405  50 V 35,976                                225,013                                      4.0   0.11     A6-BHM           6.2 1405  50 V 35,266                                231,142                                      4.0   0.11     A6-BHM           6.5 1405  50 V 34,207                                235,846                                      4.1   0.12     A6-BHM           6.8 1405  50 V 33,375                                241,100                                      4.9   0.15     A6-BHM           5.0 1360  50 V 43,797                                219,218                                      8.34  0.19     A6-BHM           5.0 1440  50 V 39,964                                221,680                                      4.96  0.12     A6-BHM           5.0 1360  70 V 39,305                                198,020                                      12.75 0.32     A6-BHM           5.0 1440  70 V 36,389                                200,869                                      7.64  0.21     B8-BHM           5.0 1440  50 V 34,053                                184,366                                      5.93  0.18     B8-BHM           5.0 1440  70 V 31,438                                169,355                                      12.81 0.41     B8-BHM           5.0 1360  50 V 36,563                                184,671                                      10.74 0.29     B8-BHM           5.0 1360  70 V 33,585                                169,258                                      24.58 0.74     A8 BHM           5.0 1360  70 V 32,281                                161,223                                      9.12  0.28     A8-BHM           5.0 1360  50 V 35,009                                175,274                                      6.27  0.18     A8-BHM           5.0 1440  70 V 30,720                                160,195                                      7.80  0.26     A8-BHM           5.0 1440  50 V 33,170                                173,240                                      4.62  0.14     __________________________________________________________________________

In general, as exemplified by the foregoing examples and as illustrated in FIG. 16, the present invention comprises a process for making, from chemically reduced basic lot powders of tantalum, a finely divided form of that powder with characteristics, including particle size and particle size distribution, by which the resultant powder is particularly well adapted to making sintered porous bodies, such as capacitor electrodes, with improved characteristics. This process is also thought to be useful for achieving similar improvements in the final particle size and particle size distribution of any metal powder, the pre-treated form of which comprises agglomerates of smaller particles. This includes, for example, the finished powder identified as "product" as well as the agglomerated by-product identified as "scrap" in the conventional process illustrated in FIG. 15.

As compared to the process illustrated in FIG. 16, other alternative embodiments encompass similar processes wherein the comminution precedes essentially any heat treatment step, either directly or indirectly.

The present invention is particularly useful for sizing an improved tantalum powder as specifically described above. However, although illustrated and described herein with reference: to certain specific embodiments, the present invention is nevertheless not intended to be limited to the details shown. Rather, various modifications may be made in the details within the scope and range of equivalents of the appended claims and without departing from the spirit of the invention. 

What is claimed:
 1. A process for preparing a tantalum powder wherein a basic lot powder of tantalum is prepared by a reduction step followed by water wash, acid leach, and drying steps prior to heat treating, said basic lot powder of tantalum having basic lot agglomerates comprised of individual powder particles, the improvement comprising:subjecting said basic lot powder to a deagglomeration step between said reduction and heat treat steps, said deagglomeration step being continued until the deagglomerated product has a size distribution such that the product of Volume Mean Diameter, MV in microns, times specific surface area, BET in m² /g, is below about
 25. 2. The process of claim 1 wherein said comminuting is continued until said comminuted product has comminuted agglomerate sizes from about 0.01 to about 20 micrometers.
 3. The process of claim 1 wherein said comminuting is continued until said comminuted agglomerate product size distribution has a D10 value less than about 2.5 micrometers.
 4. The process of claim 1 wherein said comminuting is continued until said comminuted agglomerate product size distribution has a D90 value less than about 50 micrometers.
 5. The process of claim 1 wherein said comminuted agglomerate size distribution has a D10 value less than about 2.5 and a D90 value less than about 50 micrometers.
 6. The process of claim 1 wherein said comminuted agglomerate size distribution is substantially unimodal.
 7. The process of claim 1 wherein said size distribution has a median comminuted agglomerate size of up to about 10 micrometers.
 8. The process of claim 1 wherein said comminuting step is performed by mixing said tantalum powder with a liquid and grinding said tantalum powder and liquid mixture using a high-shear mixing apparatus.
 9. The process of claim 8 wherein said liquid comprises water.
 10. The process of claim 1 wherein said comminuting step is performed using an impact mill apparatus.
 11. The process of claim 10 further comprising, before said comminuting step, reacting said tantalum powder with hydrogen.
 12. The process of claim 1 wherein said comminuting step is performed using a ball mill apparatus.
 13. The process of claim 12 further comprising, before said comminuting step, reacting said tantalum powder with hydrogen.
 14. The process of claim 1 wherein said comminuting step is performed using an ultrasonic mill apparatus.
 15. The process of claim 14 further comprising, before said comminuting step, reacting said tantalum powder with hydrogen.
 16. The process of claim 1 wherein said basic lot powder of tantalum is first produced by reducing a tantalum salt with a reducing agent, said process further including, after said comminuting step, the steps of heat treating, deoxidizing, leaching, and drying said comminuted powder.
 17. The process of claim 16 wherein said tantalum salt comprises K₂ TaF₇.
 18. The process of claim 16 wherein said reducing agent is selected from the group consisting of sodium, potassium, magnesium, calcium, and hydrogen.
 19. The process of claim 1, further comprising, after said comminuting step, heat treating said sized tantalum powder to form a heat treated tantalum powder having heat treated agglomerates.
 20. The process of claim 19, further comprising, after said heat treating step, deoxidizing said heat treated tantalum powder to form a heat treated and deoxidized agglomerated powder having heat treated and deoxidized agglomerates.
 21. The process of claim 19 wherein said heat treating step is performed at a temperature of from about 800° C. to about 1600° C.
 22. The process of claim 20 further comprising the step of screening said heat treated and deoxidized tantalum powder to yield a tantalum powder having a substantially unimodal heat treated and deoxidized agglomerate size distribution.
 23. The process of claim 22 wherein said substantially unimodal agglomerate size distribution ranges from about 30 to about 500 micrometers.
 24. The process of claim 20 wherein said heat treated and deoxidized agglomerated powder has a size distribution with a median agglomerate size of about 150 to about 250 micrometers.
 25. A tantalum powder produced in accordance with the process of claim
 1. 26. A tantalum powder produced in accordance with the process of claim
 6. 27. A tantalum powder produced in accordance with the process of claim
 14. 28. A tantalum powder produced in accordance with the process of claim
 22. 29. A comminuted tantalum powder having comminuted agglomerate particles wherein the product of the Volume Mean Diameter, MV in microns, times the specific surface area, BET in m² /g, is in the range below about
 25. 30. The comminuted tantalum powder of claim 29 having a comminuted agglomerate size distribution with a D10 value less than about 2.5 micrometers.
 31. The comminuted tantalum powder of claim 29 having a comminuted agglomerate size distribution with a D90 value less than about 20 micrometers.
 32. The comminuted powder of claim 29 having a comminuted agglomerate size distribution with a D10 value less than about 2.5 and a D90 value less than about 20 micrometers.
 33. A heat treated tantalum powder having heat treated agglomerate particles wherein the product of Volume Mean Diameter of the heat treated agglomerates, MV in microns, times the specific surface area, BET in m² /g, is in the range from about 90 to about 250 and BET is greater than about 0.7 m² /g.
 34. The heat treated tantalum powder of claim 33 having a heat treated agglomerate size distribution with a D10 value less than about
 45. 35. The heat treated tantalum powder of claim 33 having a heat treated agglomerate size distribution with a D90 value less than about 350 micrometers.
 36. The heat treated tantalum powder of claim 33 having a heat treated agglomerate size distribution with a D10 value less than about 45 and a D90 value less than about
 350. 37. A heat treated and deoxidized tantalum powder having heat treated and deoxidized agglomerate particles wherein the product of the heat treated and deoxidized agglomerate Volume Mean Diameter, MV in microns, times the specific surface area, BET in m² /g, is in the range from about 90 to about 250 and BET is greater than about 0.7 m² /g.
 38. The heat treated and deoxidized tantalum powder of claim 37 having a heat treated and deoxidized agglomerate size distribution with a D10 value less than about
 45. 39. The heat treated and deoxidized tantalum powder of claim 37 having a heat treated and deoxidized agglomerate size distribution with a D90 value less than about 350 micrometers.
 40. The heat treated and deoxidized tantalum powder of claim 37 having a heat treated and deoxidized agglomerate size distribution with a D10 value less than about 45 and a D90 value less than about
 350. 41. A comminuted basic lot powder of tantalum having comminuted agglomerate particles wherein the ratio of the Scott Bulk Density in g/in³ :BET Surface Area in m² /g is in the range from about 20 to about
 35. 42. A comminuted tantalum powder as recited in claim 29, wherein after heat treating and deoxidizing, said tantalum powder has heat treated and deoxidized agglomerate particles wherein the Scott Bulk Density in g/in³ :BET Surface Area in m² /g ratio is in the range from about 38 to about 50 and BET is greater than 0.86 m² /g.
 43. A comminuted tantalum powder as recited in claim 29, wherein after heat treating and deoxidizing, said tantalum powder has heat treated and deoxidized agglomerate particles wherein the Die Fill Rate in mg/s:BET Surface Area in m² /g ratio is in the range from about 66 to about 160 for powders with BET greater than 0.86 m² /g.
 44. A comminuted tantalum powder as recited in claim 29, wherein after heat treating and deoxidizing, said tantalum powder has heat treated and deoxidized agglomerate particles wherein the Die Fill Rate in mg/s:BET Surface Area in m² /g ratio after screening to +500 mesh is in the range from about 350 to about 700 for powders with BET greater than 0.86 m² /g.
 45. A comminuted tantalum powder adapted to be heat treated and deoxidized into a final tantalum powder useful for the manufacture of capacitors, said powder comprising comminuted agglomerate particles having a substantially unimodal agglomerate size distribution.
 46. A comminuted tantalum powder adapted to be heat treated into a final tantalum powder as recited in claim 45 wherein said comminuted agglomerates have a narrow agglomerate size distribution ranging from about 0.01 to 20 micrometers.
 47. A comminuted tantalum powder adapted to be heat treated into a final tantalum powder as recited in claim 46 wherein said comminuted agglomerates have a comminuted agglomerate size distribution with a median comminuted agglomerate size of about 3-5 micrometers.
 48. A tantalum powder useful for the manufacture of capacitors having (a) a substantially unimodal agglomerate size distribution, (b) a narrow agglomerate size distribution ranging from about 30 to 500 micrometers, and (c) an agglomerate size distribution with a median agglomerate size of about 150 to about 250 micrometers.
 49. A process for preparing a tantalum powder having a reduced size distribution by reducing a tantalum salt to produce a tantalum basic lot powder of tantalum by reduction followed by water washing, acid leaching and drying prior to heat treating, the improvement comprising:subjecting said basic lot powder of tantalum having individual powder particles forming basic lot agglomerates to a high-shear deagglomeration step between reduction and heat treat steps to achieve a sized tantalum powder having comminuted agglomerates with a size distribution having a Volume Mean Diameter, MV in microns, times specific surface area, BET in m² /g, in the range up to about
 25. 50. A method of making a tantalum powder having a limited particle size distribution from a a basic lot powder of tantalum comprising agglomerates of smaller particles prepared by reduction, water wash, acid leach and drying steps prior to heat treating said process comprising, between said reduction and heat treating steps, mechanically deagglomerating said basic lot powder to form an intermediate product having a preselected Volume Mean Diameter, MV in microns, times the specific surface area, BET in m² /g, and subsequently thermally agglomerating said intermediate product and crushing such thermally agglomerated intermediate product.
 51. In a process for producing a tantalum powder comprising reducing a tantalum salt with a reducing agent to produce a tantalum powder followed by water washing, acid leaching, drying, heat treating, crushing, deoxidation, leaching, drying and screening the tantalum powder, the improvement comprising deagglomerating the tantalum prior to said heat treating. 